D32N (p.Asp32Asn) variant of FGG (Fibrinogen gamma chain)
D32N (p.Asp32Asn) in FGG (Fibrinogen gamma chain) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data and structural context.
D32N (p.Asp32Asn) variant details
- p.Asp32Asn
- NCI-TCGA Cosmic COSV6019
- cosmic curated COSV60196
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.432
- REVEL 0.26
- CADD 25.20
- PolyPhen-2 0.39
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available